@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP86955.RAWCsZMf5AwxJD3jOWhlVAlnari6fx7PCuJ0iqCcZaE8g> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP86955.RAWCsZMf5AwxJD3jOWhlVAlnari6fx7PCuJ0iqCcZaE8g130_head {
  this: np:hasAssertion dgn-np:NP86955.RAWCsZMf5AwxJD3jOWhlVAlnari6fx7PCuJ0iqCcZaE8g130_assertion;
    np:hasProvenance dgn-np:NP86955.RAWCsZMf5AwxJD3jOWhlVAlnari6fx7PCuJ0iqCcZaE8g130_provenance;
    np:hasPublicationInfo dgn-np:NP86955.RAWCsZMf5AwxJD3jOWhlVAlnari6fx7PCuJ0iqCcZaE8g130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP86955.RAWCsZMf5AwxJD3jOWhlVAlnari6fx7PCuJ0iqCcZaE8g130_assertion a np:Assertion .
  
  dgn-np:NP86955.RAWCsZMf5AwxJD3jOWhlVAlnari6fx7PCuJ0iqCcZaE8g130_provenance a np:Provenance .
  
  dgn-np:NP86955.RAWCsZMf5AwxJD3jOWhlVAlnari6fx7PCuJ0iqCcZaE8g130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP86955.RAWCsZMf5AwxJD3jOWhlVAlnari6fx7PCuJ0iqCcZaE8g130_assertion {
  miriam-gene:2944 a ncit:C16612 .
  
  lld:C0086543 a ncit:C7057 .
  
  dgn-gda:DGN409dc803914b5ea98ebdf083feb298ee sio:SIO_000628 miriam-gene:2944, lld:C0086543;
    a sio:SIO_001122 .
}

dgn-np:NP86955.RAWCsZMf5AwxJD3jOWhlVAlnari6fx7PCuJ0iqCcZaE8g130_provenance {
  dgn-np:NP86955.RAWCsZMf5AwxJD3jOWhlVAlnari6fx7PCuJ0iqCcZaE8g130_assertion dcterms:description
      "[The present meta-analysis suggested that GSTM1 and GSTT1 null genotypes are associated with increased risk for senile cataract in Asian populations but not in Caucasian populations. Given the limited sample size, the finding on GST polymorphisms merits further investigation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
    sio:SIO_000772 miriam-pubmed:20574021;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^xsd:date .
  
  dgn-void:source_evidence_literature a eco:ECO_0000212;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}

dgn-np:NP86955.RAWCsZMf5AwxJD3jOWhlVAlnari6fx7PCuJ0iqCcZaE8g130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:43+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
    dcterms:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
      <http://orcid.org/0000-0002-9383-528X>, <http://orcid.org/0000-0003-0169-8159>, <http://orcid.org/0000-0003-1244-7654>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}